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RETRACTED: MicroRNA-374a Governs Aggressive Cell Behaviors of Glioma by Targeting Prokineticin 2 (Retracted Article)
被引:0
|作者:
Zhang, Ye
[1
]
Zhang, Rui
[2
]
Sui, Rui
[1
]
Chen, Yi
[1
]
Liang, Haiyang
[1
]
Shi, Ji
[1
]
Piao, Haozhe
[1
]
机构:
[1] China Med Univ, Canc Hosp, Dept Neurosurg, Liaoning Canc Hosp & Inst, 44 Xiaoheyan Rd, Shenyang 110042, Liaoning, Peoples R China
[2] China Med Univ, Dept Colorectal Surg, Canc Hosp, Liaoning Canc Hosp & Inst, Shenyang, Liaoning, Peoples R China
关键词:
miR-374a;
Prok2;
glioma;
tumor suppressor;
invasion;
MIR-374A PROMOTES;
MOLECULAR MARKERS;
PROLIFERATION;
ONCOGENE;
CANCER;
RELEVANCE;
INVASION;
GENOMICS;
D O I:
暂无
中图分类号:
R73 [肿瘤学];
学科分类号:
100214 ;
摘要:
MicroRNA-374a has been abnormally expressed in several cancer types; however, its role in glioma remains unclear. Therefore, we aimed to investigate whether microR-374a participated in the progression of glioma. Expression of microR-374a in glioma cell lines and normal cell line was measured by quantitative real-time polymerase chain reaction. Luciferase reporter assay and Western blot were used to detect the targets of microR-374a. In vitro functional experiments were conducted to investigate the biological role of microR-374a. Low expression of microR-374a was found in glioma cell lines. Prokineticin 2 was identified as a direct target of microR-374a in glioma. Investigations on the mechanisms related to glioma progression showed that microR-374a inhibited glioma cell proliferation, cell cycle progression, and cell invasion through targeting Prokineticin 2. Taken together, these results revealed that microR-374a functions as tumor suppressor by targeting Prokineticin 2, suggesting it might be a novel therapeutic target for glioma.
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页数:7
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